The following data is part of a premarket notification filed by Philips Medizinsysteme Boblingen Gmbh with the FDA for The Philips Mp20,mp30,mp40,mp50,mp60,mp70,mp80 And Mp90 Intellivue Atient Monitors.
Device ID | K060541 |
510k Number | K060541 |
Device Name: | THE PHILIPS MP20,MP30,MP40,MP50,MP60,MP70,MP80 AND MP90 INTELLIVUE ATIENT MONITORS |
Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
Applicant | PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH HEWLETT PACKARD STR. 2 Boblingen, DE D 71034 |
Contact | Herbert Van Dyk |
Correspondent | Herbert Van Dyk PHILIPS MEDIZINSYSTEME BOBLINGEN GMBH HEWLETT PACKARD STR. 2 Boblingen, DE D 71034 |
Product Code | MHX |
Subsequent Product Code | BZQ |
Subsequent Product Code | CBQ |
Subsequent Product Code | CBR |
Subsequent Product Code | CBS |
Subsequent Product Code | CCK |
Subsequent Product Code | CCL |
Subsequent Product Code | NHO |
Subsequent Product Code | NHP |
Subsequent Product Code | NHQ |
CFR Regulation Number | 870.1025 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-03-01 |
Decision Date | 2006-03-24 |
Summary: | summary |